Study S002794
A Single- and Multiple-Ascending Dose Study in Healthy Subjects to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HS-20094
Registration
Registered primary outcomes
- Incidence of adverse event (AE), serious adverse event (SAE), AE leading to study discontinuation, AE severity and relation with study drug [Time of Inform Consent Form to Day 29 (SAD) or Day 50 (MAD)]
Linked records (0)
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